The Berkeley biotech trying to do something the drug industry mostly gave up on: make a cyclic peptide that binds like an antibody, then get it to survive being swallowed.
The logo is a teal square with a single white "I." Simple mark, immodest goal: rewrite how hard-to-drug proteins get drugged - one swallowed peptide at a time.
Here is a fact about modern medicine that turns out to be inconvenient. The most precise drugs we have - antibodies, the biologics that hit a single target and leave the rest of the body alone - almost all have to be injected or infused. They are large, they are fragile, and the human gut is very good at destroying large, fragile things. So the most surgical medicines arrive by the least convenient route.
On the other end sit small molecules: cheap, oral, easy to make, and able to slip inside cells. Their problem is the opposite. They are small enough to go anywhere but often too small to grip the flat, sprawling surfaces where two proteins meet. Those protein-protein interactions are where a lot of disease lives, and the industry spent years calling them "undruggable," which in drug discovery is less a scientific claim than an admission of defeat.
Insamo is one of a handful of companies betting the escape hatch is a molecule in the middle: the macrocyclic peptide. A ring of amino acids big enough to grab a protein like an antibody does, engineered to be stable and greasy enough to cross a cell membrane - and, ideally, sturdy enough to be taken as a pill. It is a genuinely hard chemistry problem. Membrane permeability and antibody-like binding tend to pull in opposite directions, and finding the rare molecule that does both by hand is slow, expensive work.
Insamo's answer is to stop doing it by hand. The company - spun out of UC Berkeley and now housed at the university's Bakar Labs incubator - has built a platform that runs the search as an automated loop: design a batch of candidates with machine learning, synthesize them with parallel chemistry, test them with high-throughput molecular biology, then feed the results back into the model and go again. Each turn of the loop produces data. Enough turns, the company says, produces trillions of proprietary experimental data points - the kind of dataset that only exists if you generate it yourself.
That is the quiet insight underneath the science. The competitive advantage is not really the model; anyone can fine-tune a model. It is the data, and the only way to get this particular data is to run the experiments. Insamo is building a wet lab that behaves a bit like a search engine, indexing chemical space one measured molecule at a time.
Machine learning models propose candidate macrocycles, steering the search toward molecules that could bind tightly and still cross a membrane.
Candidates are synthesized in parallel, so a design idea becomes a physical, testable molecule quickly rather than one at a time.
Molecular-biology assays test binding and behavior at scale, generating the proprietary data that trains the next round of designs.
An integrated system pairing ML design, high-throughput molecular biology, and parallel chemistry to run automated design-synthesize-test cycles at scale.
Orally available cyclic peptides engineered to cross cell membranes while keeping antibody-like binding affinity - designed to replace injected biologics.
The platform aims to generate treatment candidates from scratch using only a small sample of target material, including targets long considered undruggable.
Insamo's founding team carries an unusually deep pedigree for a company this young - training that ran through two of the most influential protein and peptide labs in the world: David Baker's at the University of Washington and Hiroaki Suga's at the University of Tokyo.
Leads Insamo's strategy and buildout, pairing the science with a commercial plan to turn the platform into medicines.
Chief Scientific Officer, steering the peptide chemistry and molecular-biology science at the core of the platform.
Chief Operating Officer, running the operations that keep the design-synthesize-test loop turning across two sites.
Insamo emerged from stealth in February 2024 with $12 million in seed funding. What stands out is not the number but the room: a deep-tech fund, a specialist biotech fund, and a big pharma's venture arm all wrote checks into the same round. When investors that different agree, it usually means they are backing a working platform, not just a slide.
As part of the financing, Matt Hershenson of Playground Global and Corey Goodman, Ph.D. of venBio joined Insamo's board of directors.
MRL Ventures Fund is the corporate venture arm of Merck & Co. - a strategic vote of confidence in the peptide platform.
Craven, Passioura, and McIntyre begin building the platform, spinning the company out of the university and into Bakar Labs.
Insamo emerges from stealth with seed funding led by Playground Global, venBio, and Merck's MRL Ventures Fund.
Matt Hershenson (Playground Global) and Corey Goodman, Ph.D. (venBio) join the board of directors.